Technical Field
[0001] This invention relates to coated optical fibers and to a method of making same. More
particularly, the invention relates to an optical fiber having inner and outer layers
of curable coating materials that are individually cured by radiation at different
wavelengths of the electromagnetic spectrum.
Background of the Invention
[0002] In the manufacture of optical fiber, a glass preform rod is suspended vertically
and moved into a furnace at a controlled rate. The preform softens in the furnace
and a glass fiber (also referred to as an optical fiber) is drawn freely from the
molten end of the preform rod by a capstan located at the base of a draw tower.
[0003] Because the surface of the glass fiber is susceptible to damage caused by abrasion,
it is necessary to coat the fiber after it is drawn but before it comes into contact
with any surface. Inasmuch as the application of a coating material must not damage
the glass surface, the coating material is applied in a liquid state. Once applied,
the coating material must solidify before the glass fiber reaches the capstan. This
is typically accomplished within a brief time interval by photocuring -- a process
in which the liquid coating material is converted to a solid by exposure to electromagnetic
radiation.
[0004] Those optical fiber performance properties which are affected most by the coating
material are strength and transmission loss. Coating defects which may expose the
optical fiber to subsequent damage arise primarily from improper application of the
coating material. Defects such as large bubbles or voids, non-concentric coatings
with unacceptably thin regions, or intermittent coatings must be prevented. Intermittent
coating is overcome by insuring that the fiber is suitably cool at its point of entry
into the coating applicator to avoid coating flow instabilities. Coating concentricity
can be monitored and adjustments made to maintain an acceptable value.
[0005] Optical fibers are susceptible to a transmission loss mechanism known as microbending.
Because the fibers are thin and flexible, they are readily bent when subjected to
mechanical stresses such as those encountered during handling or exposure to varying
temperature environments. If the stresses placed on the fiber result in a random bending
distortion of the fiber axis with periodic components in the millimeter range, light
rays, or modes, propagating in the fiber may escape from the core. These losses, termed
microbending losses, may be very large, often many times the intrinsic loss of the
fiber itself. The optical fiber must be isolated from stresses which cause microbending.
The properties of the optical fiber coating material play a major role in providing
this isolation -- coating geometry, modulus and thermal expansion coefficient being
the most important factors.
[0006] Typically, two layers of coating materials are applied to the drawn optical fiber,
and two different kinds of coating materials are used. An inner layer, referred to
as a primary coating material, is applied to the optical glass fiber. And an outer
layer, referred to as a secondary coating material, is applied to the primary coating
material. Usually, the secondary coating material has a relatively high modulus, e.
g. 10⁹ Pa, whereas the primary coating material has a relatively low modulus such
as, for example, 10⁶ Pa. In one arrangement, the primary and the secondary coating
materials are advantageously applied at substantially the same time. Such an arrangement
is referred to as a "wet/wet" system because the secondary coating is applied directly
to a non-cured primary coating. See for example, U.S. Patent 4,474,830 in which both
the inner and the outer layers of coating materials are cured beginning from the outside
progressing inwardly. The primary and secondary coating materials comprise materials
which are cured by exposure to electromagnetic radiation. The coating materials are
characterized by a photoactive region, i.e., a range of wavelengths within the electromagnetic
spectrum which are absorbed by the liquid coating material and cause it to change
to a solid.
[0007] It is important that both coatings be fully cured and that the curing process proceed
rapidly -- a concern that has been addressed in the prior art by a process in which
the primary coating material is applied to the glass fiber and cured after which a
secondary coating material is applied and cured. This process suffers from the drawback
that multiple coating applicators and curing stations are required which increases
cost, complexity and opportunity for equipment malfunction. U.S. Patent 5,015,068
discloses the application of both primary and secondary coatings at nearly the same
time, but still requires two curing stations -- the first one using visible light
to cure the primary coating and the second one using ultraviolet light to cure the
secondary coating. By curing the primary coating first, the problem that the secondary
coating becomes opaque to curing wavelengths, and thus retards the cure of the primary
coating, is overcome. However, two curing stations are required which add to the cost
and complexity of the overall system. Further, use of a photoinitiator that responds
to radiation in the visible portion of the electromagnetic spectrum leads to certain
difficulties in handling of the primary coating material.
[0008] Recently it has been learned that the curing speed of the primary coating material
is much slower at high temperatures, and that substantial heat is released when the
secondary coating material changes from a liquid into a solid.
[0009] What is needed, and seemingly what is not disclosed in the prior art, is a method
for curing a wet/wet coating system which only uses a single radiation source and
is capable of being integrated with present manufacturing arrangements for drawing
optical fiber from a preform.
Summary of the Invention
[0010] The foregoing problems of the prior art have been solved by a method of making a
coated optical fiber in which primary and secondary coating materials are applied
to a glass fiber and then simultaneously cured. The primary coating material encloses
and engages the glass fiber while the secondary coating material encloses and engages
the primary coating material. A photoinitiator is added to each of the primary and
secondary coating materials which respond to electromagnetic radiation from one or
more curing lamps having identical emission spectra; but, the photoinitiator added
to the primary coating is selected to be substantially more responsive to the radiation
than the photoinitiator added to the secondary coating material.
In one illustrative embodiment, the photoinitiator added to the primary coating material
responds to a first wavelength region of the electromagnetic emission spectrum of
the curing lamp, while the photoinitiator added to the secondary coating material
responds to a second wavelength region of its electromagnetic emission spectrum. In
this embodiment, the radiated energy in the first region is substantially greater
than the radiated energy in the second region.
In another illustrative embodiment, the photoinitiators added to the primary and secondary
coating materials respond to electromagnetic energy in substantially the same wavelength
region of the electromagnetic spectrum; however, an increased concentration is used
with the primary coating material to accelerate curing. In the illustrative embodiments
of the invention, the first and second spectral regions reside within the ultraviolet
portion of the electromagnetic spectrum. The typical advantages of standardization
accompany the use of curing lamps having the same spectral emission characteristic.
[0011] Other features of the present invention will be more readily understood from the
following detailed description of specific embodiments thereof when read in conjunction
with the accompanying drawings, in which:
FIG. 1 is a schematic view of a manufacturing line for drawing optical fiber from
a preform in accordance with the present invention;
FIG. 2 is an end view in section of a dual-coated optical fiber;
FIG. 3 is a histogram which shows the emission output of a commercially-available
curing lamp which is suitable for use in the present invention;
FIG. 4 is a graph depicting a plot of absorbance vs. wavelength of a photoinitiator
which responds to radiation in the 386 nanometer region of the electromagnetic spectrum;
FIG. 5 is a graph depicting a plot of absorbance vs. wavelength of two concentrations
of a photoinitiator which responds to radiation in the 330 nanometer region of the
electromagnetic spectrum;
FIG. 6 is a graph depicting in-situ modulus as a function of incident energy for different
combinations of primary and secondary photoinitiators; and FIG. 7 is a graph depicting
pullout force as a function of incident energy for different combinations of primary
and secondary photoinitiators.
Detailed Description
[0012] Referring now to FIG. 1, there is shown an apparatus which is designated generally
by the numeral 20 and in which is used to draw optical fiber 21 from a specially prepared
cylindrical preform 22 and for then coating the drawn fiber. The optical fiber 21
is formed by locally and symmetrically heating the preform 22, typically 15 to 40
mm in diameter and 60 cm in length, to a temperature of about 2000XC. As the preform
is fed into and through a furnace 23, fiber 21 is drawn from the molten material.
[0013] As can be seen in FIG. 1, the elements of the draw system include the furnace 23
wherein the preform is drawn down to the fiber size after which the fiber 21 is pulled
from a heat zone therein. The diameter of the fiber 21 is measured by a device 24
at a point shortly after the fiber is formed and this measured value becomes an input
into a control system. Within the control system, the measured diameter is compared
to the desired value and an output signal is generated to adjust the draw speed such
that the fiber diameter approaches the desired value.
[0014] After the diameter of the optical fiber 21 is measured, a protective coating system
25 (see also FIG. 2) is applied to the fiber by an apparatus 27. Preservation of fiber
strength requires the application of the protective coating, which shields newly drawn
fiber from the deleterious effects of the atmosphere. This coating system must be
applied in a manner that does not damage the surface of the fiber 21 and such that
the fiber has a predetermined diameter and is protected from abrasion during subsequent
manufacturing operations, installation and service. Minimizing attenuation requires
the selection of a suitable coating material and a controlled application of it to
the fiber. Such a coating apparatus may be one such as described in previously identified
U. S. Patent 4,474,830. Minimizing diameter variation which in turn minimizes the
losses due to misalignment at connector and splice points requires careful design
of the draw system and the continuous monitoring and control of the fiber diameter
during the drawing and the coating steps of the process. Then, the coated fiber 21
is passed through a centering gauge 28.
[0015] After the coating materials have been applied to the drawn fiber, the coating materials
must be cured. Accordingly, the optical fiber having the coating materials thereon
is passed through a device 30 for curing the coating system and a device 32 for measuring
the outer diameter of the coated fiber. Afterwards, it is moved through a capstan
34 and is spooled for testing and storage prior to subsequent cable operations.
[0016] In the apparatus 27, the coating system 25 comprising two coating materials are applied
to the optical fiber. The coating system 25 includes an inner layer 42 (see FIG. 2),
which often is referred to as a primary coating layer, and an outer layer 44, which
often is referred to as a secondary coating material. The coating material of the
inner layer, which has a substantially lower modulus than that of the outer layer,
is such that it prevents microbending of the optical glass fiber. On the other hand,
the higher modulus outer layer provides mechanical protection for the drawn glass
fiber.
[0017] Each of the coating materials is curable by being exposed to an appropriate portion
of the electromagnetic spectrum. Such cure is accomplished via a reactive polymer
that can polymerize by free radical polymerization. Generally, each of the coating
materials includes an oligomer, a diluent and a photoinitiator. Also included may
be additives such as, for example, antioxidants, adhesion promoters, ultraviolet (UV)
light stabilizers, surfactants and shelf life stabilizers. Of particular interest
in connection with the present invention are the photoinitiators which, in response
to electromagnetic radiation within a narrow range of wavelengths, cause the coating
material to change from a liquid to a solid. This change of state is accompanied by
the release of heat which affects on the speed at which the coating material changes
state. Photoinitiators may be customized to respond (i.e., initiate free radical polymerization)
in different regions of the electromagnetic spectrum --typically in the ultraviolet
(UV) region.
[0018] It has been learned that the equilibrium modulus of a UV-cured coating is directly
proportional to the crosslink density, and that the equilibrium modulus of a coating
decreases with increasing cure temperature. See, e.g., "The Effects of Cure Temperature
on the Thermomechanical Properties of UV Curable Coatings,"
Polymer Engineering and Science, Vol 29, No. 17, Sept., 1989 (pages 1165-1168). Therefore, it is highly desirable
to cure the polymer coatings at a relatively low temperature (e.g., 20°C rather than
200°C). Furthermore, approximately 70% of the heat (temperature rise) associated with
the curing process is generated by the reaction itself while only about 30% comes
from the curing lamp. Accordingly, it is most important to accelerate curing of the
inner (primary) coating material before the heat of reaction --generated by the outer
(secondary) coating material as it polymerizes -- adversely affects its curing rate.
Embodiment I - Different Photoactive Regions
[0019] Referring now to the end view of a dual-coated optical fiber shown in FIG. 2, the
coating material of primary layer 42 is formulated such that it cures upon exposure
to different region of the electromagnetic spectrum than does the secondary layer
44. The region is typically designated by a wavelength at about the center the region.
For example, the wavelength region used to initiate free radical polymerization of
the primary coating material is designated λ
p, and the wavelength region used to initiate free radical polymerization of the secondary
coating material is designated λ
s. One way to achieve simultaneous curing of the primary and secondary coating materials
using the emission spectrum of a single source of electromagnetic radiation is to
use two identical curing lamps which individually emit λ
p and λ
s, and then adding a "screen" in the top lamp of curing station 30 (see FIG. 1) to
block a portion of λ
s until the primary coating has been partially or fully cured. A convenient implementation
of such an arrangement is a vertical stacking of two curing lamps and two glass tubes
(screens). The top glass tube is made from borosilicate glass, which attenuates electromagnetic
radiation having wavelengths of 350 nm or less; while the bottom glass tube is made
from quartz glass, which is virtually transparent. Naturally, the photoinitiator associated
with the primary coating would respond to wavelengths that are greater than 350 nm,
while the photoinitiator associated with the secondary coating would respond to wavelengths
that are less than 350 nm. A dual-coated optical fiber moves through these glass tubes
and the curing of its primary coating is accelerated with respect to the secondary
coating. A tube diameter of two inches, is acceptable for most applications, but the
wall thickness of the borosilicate glass is empirically determined based on the amount
of attenuation of λ
s that is desired. Nevertheless, it is desirable to further improve this arrangement
by eliminating the need for different glass tubes.
[0020] FIG. 3 is a histogram which shows the emission output of a curing lamp which is suitable
for use in the present invention. The specific output spectrum shown is produced by
a non-mercury "D" lamp which is commercially-available from Fusion Systems Corporation.
In particular, advantage is taken of the fact that emission in the region λ = 386
nanometers (nm) is substantially greater than emission in other regions of its spectrum.
Accordingly, a photoinitiator that responds to electromagnetic radiation in the λ
= 386 nm region is selected for use with the primary coating material so that it will
cure at a faster rate than the secondary coating material -- which has a photoinitiator
that responds to electromagnetic radiation in another wavelength region. In this regard,
a photoinitiator having maximum absorbance at 382 nm is chemically known as 2,4,6-Trimethylbenzoyldiphenylphosphine
oxide and is suitable for use with the primary coating material. It is commercially
known as Lucirin TPO and is available from the BASF Company. FIG. 4 shows the absorbance
spectrum of Lucirin TPO in greater detail which has been specially selected to match
the emission peak of the curing lamp. Together, they cooperate to accelerate the curing
rate of the primary coating material.
[0021] Referring once again to FIG. 3, another region of the emission spectrum of the curing
lamp is selected for use in curing the secondary coating material. In this illustrative
embodiment, the wavelength region in the vicinity of 330 nm is selected because the
lamp output is substantially less in that region than in the 386 nm wavelength region.
For the secondary coating, one suitable photoinitiator is a 2-methyl--[4-(methylthio)phenyl]-2-(4morpholinyl)-1-propanone,
such as Irgacure 907, which is commercially available from the Ciba Giegy Company
and whose absorbance spectrum is shown in FIG. 5 for various concentrations. Irgacure
907 exhibits maximum absorbance at 300 nm which, it is noted, does not necessarily
coincide with any special region of the lamp's emission spectrum. Rather, it was selected
via trial and error from a lower emission region of the spectrum than the region used
for curing the primary coating material. Indeed, given the emission spectrum of the
curing lamp, it would only require a small amount of experimentation by one of ordinary
skill in the chemical art, to select acceptable photoinitiators for use with the primary
and secondary coating materials. By thus accelerating the cure of the primary coating
material before the heat released by polymerization of the secondary coating material
becomes a detrimental factor, a single radiation source can be used to simultaneously
cure both primary and secondary coating materials. Another suitable photoinitiator
which may be used in the secondary coating is a 1 - hydroxycyclohexyl phenyl ketone,
such as Irgacure 184. This photoinitiator is also commercially available from the
Ciba Geigy Company.
Embodiment II - Different Concentrations of Photoinitiator
[0022] Referring once again to FIG. 5, it is noted that the absorbance of a photoinitiator
is influenced by the concentration used -- a property that is advantageously used
in a second embodiment of the invention. Note that in the above-described Embodiment
I, the primary and secondary coatings are simultaneously applied and simultaneously
cured. In order to accelerate the curing of the primary coating vis a' vis the secondary
coating, photoinitiators operating at different wavelength regions of the same curing
lamp are selected. However, it is also possible to accelerate the curing of the primary
coating vis a' vis the secondary coating by adding different concentrations of the
same photoinitiator to the primary and secondary coating materials. Naturally, a greater
concentration is added to the primary coating material. It is further noted that different
photoinitiators may be used, each being responsive to the same wavelength region --
yet one being more responsive than the other. As shown in FIG. 5, the absorbance of
the photoinitiator is increased approximately in proportion to its concentration.
Here, concentrations of 0.001% and 0.002% are shown increasing the peak absorbance
by a factor of 2. The wellknown, practical range for photoinitiators resides between
0.5% and 5.0% by weight for most UV formulations having commercial utility.
Results
[0023] Suitable curing of an optical fiber coating is very important because one that is
improperly cured will inhibit cabling. Also, an undercured coating material frequently
emits an undesirable odor, an exhibits poor strippability, poor adhesion and poor
reliability relative to a properly cured coating. As should be evident, properly cured
coating materials for drawn optical fibers are important to the quality of the final
product. Further, the modulus of the cured material is a function of the degree of
cure. Modulus is important to the mechanical and optical performance of the optical
fiber product.
[0024] Presently, there are several methods which are used to determine the degree of cure
of optical fiber coating materials. In one method, referred to as the in-situ modulus
test, a cut is made through the coating or coating layers to the glass. A load is
applied to the optical fiber and measurements are taken as to the time during which
the load is applied to the fiber and the distance through which the optical fiber
moves. From these measurements, the modulus of the coatings can be determined. FIG.
6 is a graph depicting the results of an in-situ modulus test, performed on Embodiment
I of the present invention, as a function of incident energy for different combinations
of primary and secondary photoinitiators. (Similar results are anticipated for Embodiment
II of the invention). The dotted line results of the in-situ modulus test were obtained
using photoinitiators in the primary and secondary coating materials at appropriate
concentration levels; the photoinitiators were selected to respond to electromagnetic
radiation in the same wavelength region (

). The solid line results of the in-situ modulus test were obtained using photoinitiators
in the primary and secondary coating materials, at appropriate concentration levels,
which respond to electromagnetic radiation in two different wavelength regions (λ
p = 386 nm, and λ
s = 330 nm). The results show an approximate 40% increase in the in-situ modulus which
represents an important improvement because it enables a substantial increase in the
draw speed of the dual-coated optical fiber. These results are confirmed by the below-discussed
pullout test.
[0025] In a pullout test, a length of optical fiber is positioned in a well-known, Instron
apparatus. The force which is necessary to pull the optical fiber from the coating
material is measured. This measurement is proportional to the degree of cure. FIG.
7 is a graph depicting the results of a pullout test, performed on Embodiment I of
the present invention, as a function of incident energy for different combinations
of primary and secondary photoinitiators. (Similar results are anticipated for Embodiment
II of the invention). The dotted line results of the pullout test were obtained using
photoinitiators in the primary and secondary coating materials at appropriate concentration
levels; the photoinitiators were selected to respond to electromagnetic radiation
in the same wavelength region (

). The solid line results of the pullout test were obtained using photoinitiators
in the primary and secondary coating materials, at appropriate concentration levels,
which respond to electromagnetic radiation in two different wavelength regions (λ
p = 386 nm, and λs = 330 nm). Similar to the results of in-situ modulus testing, these
results show an approximate 40% increase in pullout force confirming that use of the
present invention provides a substantial improvement in curing rate.
[0026] Although various particular embodiments have been shown and described, it is understood
that other arrangements may be devised by those skilled in the art which will embody
the principles of the invention and fall within the spirit and scope thereof. These
other arrangements include, but are not limited to, the use of curing lamps and photoinitiators
other than disclosed herein, the use of a screen to decrease electromagnetic radiation
at wavelengths associated with the secondary coating material rather than relying
on a decreased region of radiation in the emission spectrum of the curing lamp, and
the use of the present invention in connection with processes for obtaining glass
fibers other than drawing it from a preform.
1. A method of curing a dual-coated optical fiber comprising a glass fiber 21 which is
surrounded by primary 42 and secondary 44 coating materials, said coating materials
each including a photoinitiator which responds to radiated electromagnetic energy
within a predetermined wavelength range to increase the speed at which the coating
materials cure, the method comprising the steps of:
applying the primary coating material 42 to the glass fiber 21, the material including
a first photoinitiator which is responsive to electromagnetic energy from a source
of electromagnetic radiation which comprises one or more curing lamps having substantially
identical emission spectra;
applying a secondary coating material 44 to the primary coating material 42, the
secondary coating material including a second photoinitiator which is substantially
less responsive to the the source of electromagnetic radiation than the first photoinitiator;
and
exposing the dual-coated optical fiber to the source of electromagnetic radiation
for the purpose of simultaneously curing said primary and secondary coatings; whereby
the primary coating is cured at faster rate than the secondary coating.
2. The method of claim 1 wherein the source of electromagnetic radiation emits a greater
amount of energy within a first wavelength region than in a second wavelength region,
said method further including the steps of:
selecting the first photoinitiator to be substantially more responsive to radiated
energy in the first wavelength region than the second wavelength region; and
selecting the second photoinitiator to be substantially more responsive to radiated
energy in the second wavelength region than the first wavelength region.
3. The method of claim 1 wherein the photoinitiator added to the primary coating 42 comprises
Lucirin TPO.
4. The method of claim 1 wherein the photoinitiator added to the secondary coating 44
material comprises Irgacure 907.
5. The method of claim 1 wherein the photoinitiator added to the secondary coating material
44 comprises Irgacure 184.
6. The method of claim 1 wherein the source of electromagnetic radiation includes a predetermined
wavelength region which is used for curing both primary and secondary coatings, said
method further including the step of:
selecting the first and second photoinitiators such that they both respond to electromagnetic
radiation in the predetermined wavelength region; and
selecting the concentrations of the photoinitiators applied to the primary and
secondary coatings such that the primary coating cures at a rate which is substantially
greater than rate at which the secondary coating cures.
7. The method of claim 6 wherein the predetermined wavelength region resides substantially
in the range 260-340 nm.
8. The method of claim 6 wherein the photoinitiators added to the primary and secondary
coating materials comprises Irgacure 907.
9. The method of claim 6 wherein the photoinitiators added to the primary 42 and secondary
44 coating materials comprises Irgacure 184.
10. A dual-coated optical fiber, manufactured in accordance with the following process:
drawing glass fiber 21 from a preform 22;
surrounding the drawn glass fiber with an inner coating layer 42 of material having
a first photoactive region which corresponds to a first wavelength region;
surrounding the inner coating layer with an outer coating layer 44 of material
having a second photoactive region which corresponds to a second wavelength region;
simultaneously curing the coating materials of the inner and outer layers by exposing
the dual-coated glass fiber to one or more curing lamps 30 having identical emission
spectra, said emission spectra comprising substantially greater emission in the first
wavelength region than in the second wavelength region; and
taking up the cured optical fiber.